Cóvid-safer events in Chicago this week and next!
All of them will have at least one of our air purifiers. Some will also require masks!!
Cóvid safety is easy when we do it together 🩵🩵🩵
Does anyone have recommendations for (ideally free or cheap) software for producing DJ mixes - i.e. literally just mixing one song into the next in a playlist, with a few crossfades and maybe a little beat matching? The last time I was DJing regularly we were still using CDs...
Tickets for the UK shows went on sale at 10am - *don't* wait for the time advertised below. The Bird on the Wire ticket site that's linked on the tour page will put you in a seemingly endless queue but other sites also have tickets you can buy right away.
@brokemystrings I am considering it! Chronic illness forced me to give up basically everything outside of my day job for like 2 years and now I'm trying to figure out which things to pick up again and how to make it fit within my current limits.
For London tickets it took me 39 mins to get to the front of the queue at Bird on the Wire (things might have slowed down now though) but you can get straight through to buy them here: https://t.co/99AfbzBqAf
@bennessb Yeah, very different things. FB is useful for e.g. discussing symptoms/treatments with people with the same condition. But most chronic illness FB groups IME aren't engaged with wider disability politics and some even ban political discussions.
@scotjess3@actionforme@jdibon one didn't). I think how useful it is maybe depends on what treatment you've had so far. But it's useful to know you can see a doctor there who properly understands ME, whereas it's always a crapshoot on the NHS.
@scotjess3@actionforme@jdibon I used the GP service. I joined their waiting list (which is long) while I was awaiting a diagnosis on the NHS. In the end I got the NHS one first, but the ActionforME GP confirmed and properly documented my symptoms and ran through the diagnostic criteria with me (which the NHS
@Hannah_Chutzpah Sorry to hear it's hit you like this. As far as I can tell there is also zero research on how covid affects ME/CFS patients. In case of interest, @MEActNet is organising this action on 13 Sept - I'm planning to go: https://t.co/Rve8FcJ5st